机构地区:[1]北京中医药大学东直门医院,北京市100700 [2]成都大学附属医院 [3]河南省漯河市中医院 [4]河南省洛阳市第三人民医院 [5]河南省开封市中医院 [6]黑龙江中医药大学附属第二医院 [7]山东中医药大学第二附属医院
出 处:《中医杂志》2024年第11期1139-1145,共7页Journal of Traditional Chinese Medicine
基 金:北京中医药大学一流学科建设引导项目;北京中医药大学课程思政建设专项(KCSZZD-06);北京中医药大学2023年度基本科研业务费项目(2023-BUCMXJKY009)。
摘 要:目的评价百蕊颗粒治疗急性咽炎风热证的临床疗效及安全性。方法采用多中心、双盲、双模拟、随机对照试验方法,选取来自7个中心的162例急性咽炎风热证患者,各中心按照试验组与对照组2∶1的比例分组。试验组108例应用百蕊颗粒+热炎宁颗粒模拟剂口服,对照组54例应用热炎宁颗粒+百蕊颗粒模拟剂口服,疗程5天,并于第6天随访。分别采用全分析集(FAS)和符合方案集(PPS)进行分析。主要疗效指标为治疗5天后咽痛消失率;次要疗效指标为治疗3天后咽痛消失率,治疗前、治疗每天及第6天随访时咽痛视觉模拟评分法(VAS)评分,治疗前及第6天随访时进行中医证候评分,并于第6天随访时评价中医证候疗效;记录治疗前后生命体征、血常规、尿常规、肝功能、肾功能等变化,不良事件的发生情况,进行安全分析集(SS)分析。结果本研究162例患者进入FAS和SS分析,158例(试验组105例,对照组53例)进入PPS分析。FAS分析显示,试验组治疗5天后咽痛消失率为80.56%(87/108),对照组为64.81%(35/54),两组差异有统计学意义(χ^(2)=5.10,P=0.0239);PPS分析显示,试验组患者治疗5天后咽痛消失率为80.00%(84/105),对照组为64.15%(34/53),两组差异有统计学意义(χ^(2)=4.85,P=0.0277)。FAS和SS分析均显示,两组治疗3天后咽痛消失率差异无统计学意义(P>0.05);与本组治疗前比较,两组治疗第2、3、4、5天及第6天随访时咽痛VAS评分均降低(P<0.01),但两组间各时间点比较差异无统计学意义(P>0.05);两组第6天随访时中医证候评分均低于本组治疗前,且试验组低于对照组(P<0.01);试验组中医证候疗效痊愈率、愈显率均显著高于对照组(P<0.01)。治疗前后两组患者血常规、尿常规、肝功能、肾功能差异均无统计学意义(P>0.05),均未发生严重不良事件。结论百蕊颗粒治疗急性咽炎风热证临床疗效肯定,可显著改善临床症状,且安全性好。Objective To evaluate the clinical effectiveness and safety of Bairui Granules(百蕊颗粒)in the treatment of acute pharyngitis with wind-heat syndrome.Methods A multicenter,double-blind,double-simulation,randomised controlled trial was conducted,in which 162 patients with acute pharyngitis and wind-heat syndrome from 7 centers were recruited,and each center was divided into trial group and control group on the ratio of 2∶1.In the trial group,108 cases were orally administered with Bairui Granules plus Reyanning Granules(热炎宁颗粒)simulant,and in the control group,54 cases were orally administered with Reyanning Granules plus Bairui Granules simulant for 5 days,with a follow-up visit on the 6th day.Full analysis set(FAS)analysis and per protocol set(PPS)were used for analysis,respectively.The primary efficacy index was the disappearance rate of sore throat after 5-day treatment;the secondary efficacy indexes were the disappearance rate of sore throat after 3-day treatment,as well as the visual analogue score(VAS)of sore throat before treatment,every day during the treatment,and follow-up on day 6,and the traditional Chinese medicine(TCM)syndrome score was performed before treatment and at the follow-up on day 6.The effectiveness on TCM syndrome was evaluated at the follow-up on day 6,and the changes of vital signs,blood routine,urine routine,liver functions,kidney function,the adverse events before and after the treatment were recorded,and safety analysis set(SS)was analysed.Results 162 patients entered the FAS and SS analyses,and 158 cases(105 cases in the trial group and 53 cases in the control group)entered the PPS analysis.FAS analysis showed that the disappearance rate of sore throat after 5-day treatment was 80.56%(87/108)in the trial group and 64.81%(35/54)in the control group,and the difference between groups was statistically significant(χ^(2)=5.10,P=0.0239).PPS analysis showed that the disappearance rate of sore throat after 5-day treatment was 80.00%(84/105)in the trial group and 64.15%(34/5
分 类 号:R276.1[医药卫生—中医五官科学]
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